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Showing results (541-550 of 642) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE studyDavid B Zhen, Kari G Rabe, Steven Gallinger, et al.
Cancer Research|April 17, 2010
A second genetic variant on chromosome 15q24-25.1 associates with lung cancerPengyuan Liu, Ping Yang, Xifeng Wu, et al.
Breast Cancer Research and Treatment|September 20, 2014
Outcomes of HER2-positive early breast cancer patients in the pre-trastuzumab and trastuzumab eras: a real-world multicenter observational analysis. The RETROHER studyPatrizia Vici, Laura Pizzuti, Clara Natoli, et al.
Molecular Genetics and Metabolism|October 27, 2009
Alpha-1-antitrypsin deficiency and smoking as risk factors for mismatch repair deficient colorectal cancer: a study from the colon cancer family registryNoralane M Lindor, Ping Yang, Ilonka Evans, et al.
JAMA|February 17, 2005
Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancerGraham Casey, Noralane M Lindor, Nickolas Papadopoulos, et al.
The Journal of Clinical Endocrinology and Metabolism|June 30, 2012
When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR)Elena Gianetti, Janet E Hall, Margaret G Au, et al.
The New England Journal of Medicine|May 10, 2013
Ataxia, dementia, and hypogonadotropism caused by disordered ubiquitinationDavid H Margolin, Maria Kousi, Yee-Ming Chan, et al.
Mayo Clinic Proceedings|November 13, 2001
Circulating natriuretic peptide concentrations in patients with end-stage renal disease: role of brain natriuretic peptide as a biomarker for ventricular remodelingA Cataliotti, L S Malatino, M Jougasaki, et al.
JCI Insight|January 5, 2023
Heterozygous mutations in SOX2 may cause idiopathic hypogonadotropic hypogonadism via dominant-negative mechanismsJessica Cassin, Maria I Stamou, Kimberly W Keefe, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 5, 2009
The association of tumor microsatellite instability phenotype with family history of colorectal cancerBharati Bapat, Noralane M Lindor, John Baron, et al.
Pageof 65

Showing results (541-550 of 642) with videos related to

Sort By:
Pageof 65
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE studyDavid B Zhen, Kari G Rabe, Steven Gallinger, et al.
Cancer Research|April 17, 2010
A second genetic variant on chromosome 15q24-25.1 associates with lung cancerPengyuan Liu, Ping Yang, Xifeng Wu, et al.
Breast Cancer Research and Treatment|September 20, 2014
Outcomes of HER2-positive early breast cancer patients in the pre-trastuzumab and trastuzumab eras: a real-world multicenter observational analysis. The RETROHER studyPatrizia Vici, Laura Pizzuti, Clara Natoli, et al.
Molecular Genetics and Metabolism|October 27, 2009
Alpha-1-antitrypsin deficiency and smoking as risk factors for mismatch repair deficient colorectal cancer: a study from the colon cancer family registryNoralane M Lindor, Ping Yang, Ilonka Evans, et al.
JAMA|February 17, 2005
Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancerGraham Casey, Noralane M Lindor, Nickolas Papadopoulos, et al.
The Journal of Clinical Endocrinology and Metabolism|June 30, 2012
When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR)Elena Gianetti, Janet E Hall, Margaret G Au, et al.
The New England Journal of Medicine|May 10, 2013
Ataxia, dementia, and hypogonadotropism caused by disordered ubiquitinationDavid H Margolin, Maria Kousi, Yee-Ming Chan, et al.
Mayo Clinic Proceedings|November 13, 2001
Circulating natriuretic peptide concentrations in patients with end-stage renal disease: role of brain natriuretic peptide as a biomarker for ventricular remodelingA Cataliotti, L S Malatino, M Jougasaki, et al.
JCI Insight|January 5, 2023
Heterozygous mutations in SOX2 may cause idiopathic hypogonadotropic hypogonadism via dominant-negative mechanismsJessica Cassin, Maria I Stamou, Kimberly W Keefe, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 5, 2009
The association of tumor microsatellite instability phenotype with family history of colorectal cancerBharati Bapat, Noralane M Lindor, John Baron, et al.
Pageof 65